|Publication number||US6982740 B2|
|Application number||US 09/971,749|
|Publication date||Jan 3, 2006|
|Filing date||Oct 4, 2001|
|Priority date||Nov 24, 1997|
|Also published as||US20020080248, WO2003030525A1|
|Publication number||09971749, 971749, US 6982740 B2, US 6982740B2, US-B2-6982740, US6982740 B2, US6982740B2|
|Inventors||Edwin L. Adair, Jeffrey L. Adair, Randall S. Adair|
|Original Assignee||Micro-Medical Devices, Inc.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (32), Non-Patent Citations (4), Referenced by (195), Classifications (36), Legal Events (4)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application is a continuation-in-part application of U.S. Ser. No. 09/368,246, filed on Aug. 3, 1999, now U.S. Pat. No. 6,310,642 and entitled “Reduced Area Imaging Device Incorporated Within Surgical Instruments”, which is a continuation-in-part of U.S. Ser. No. 08/976,976, filed Nov. 24, 1997, and entitled “Reduced Area Imaging Devices Incorporated Within Surgical Instruments”, now U.S. Pat. No. 5,986,693. This application is also a continuation-in-part application of U.S. Ser. No. 09/586,768, filed on Jun. 1, 2000 now U.S. Pat. No. 6,316,215 and entitled “Methods of Cancer Screening Utilizing Fluorescence Detection Techniques and Selectable Imager Charge Integration Periods”
This invention relates to solid state image sensors and associated electronics, and more particularly, to solid state image sensors which are configured to be of a minimum size, and which utilize selectable charge integration periods.
In recent years, endoscopic surgery has become the accepted standard for conducting many types of surgical procedures, both in the medical and dental arenas. The availability of imaging devices enabling a surgeon or dentist to view a particular surgical area through a small diameter endoscope which is introduced into small cavities or openings in the body results in much less patient trauma as well as many other advantages.
In many hospitals, the rod lens endoscope is still used in endoscopic surgery. The rod lens endoscope includes a very precise group of lenses in an elongate and rigid tube which are able to accurately transmit an image to a remote camera in line with the lens group. The rod lens endoscope, because of its cost of manufacture, failure rate, and requirement to be housed within a rigid and straight housing, is being increasingly replaced by solid state imaging technology which enables the image sensor to be placed at the distal tip of the investigating device. The three most common solid state image sensors include charged coupled devices (CCD), charge injection devices (CID) and photo diode arrays (PDA). In the mid-1980s, complementary metal oxide semiconductors (CMOS) were developed for industrial use. CMOS imaging devices offer improved functionality and simplified system interfacing. Furthermore, many CMOS imagers can be manufactured at a fraction of the cost of other solid state imaging technologies.
One particular advance in CMOS technology has been in the active pixel-type CMOS imagers which consist of randomly accessible pixels with an amplifier at each pixel site. One advantage of active pixel-type imagers is that the amplifier placement results in lower noise levels than CCDs or other solid state imagers. Another major advantage is that these CMOS imagers can be mass produced on standard semiconductor production lines. One particularly notable advance in the area of CMOS imagers including active pixel-type arrays is the CMOS imager described in U.S. Pat. No. 5,471,515 to Fossum, et al. This CMOS imager can incorporate a number of other different electronic controls that are usually found on multiple circuit boards of much larger size. For example, timing circuits, and special functions such as zoom and anti-jitter controls can be placed on the same circuit board containing the CMOS pixel array without significantly increasing the overall size of the host circuit board. Furthermore, this particular CMOS imager requires 100 times less power than a CCD-type imager. In short, the CMOS imager disclosed in Fossum, et al. has enabled the development of a “camera on a chip.”
Passive pixel-type CMOS imagers have also been improved so that they too can be used in an imaging device which qualifies as a “camera on a chip.” In short, the major difference between passive and active CMOS pixel arrays is that a passive pixel-type imager does not perform signal amplification at each pixel site. One example of a manufacturer which has developed a passive pixel array with performance nearly equal to known active pixel devices and being compatible with the read out circuitry disclosed in the U.S. Pat. No. 5,471,515 is VLSI Vision, Ltd., 1190 Saratoga Avenue, Suite 180, San Jose, Calif. 95129. A further description of this passive pixel device may be found in co-pending application, Ser. No. 08/976,976, entitled “Reduced Area Imaging Devices Incorporated Within Surgical Instruments,” and is hereby incorporated by reference.
In addition to the active pixel-type CMOS imager which is disclosed in U.S. Pat. No. 5,471,515, there have been developments in the industry for other solid state imagers which have resulted in the ability to have a “camera on a chip.” For example, Suni Microsystems, Inc. of Mountain View, Calif., has developed a CCD/CMOS hybrid which combines the high quality image processing of CCDs with standard CMOS circuitry construction. In short, Suni Microsystems, Inc. has modified the standard CMOS and CCD manufacturing processes to create a hybrid process providing CCD components with their own substrate which is separate from the P well and N well substrates used by the CMOS components. Accordingly, the CCD and CMOS components of the hybrid may reside on different regions of the same chip or wafer. Additionally, this hybrid is able to run on a low power source (5 volts) which is normally not possible on standard CCD imagers which require 10 to 30 volt power supplies. A brief explanation of this CCD/CMOS hybrid can be found in the article entitled “Startup Suni Bets on Integrated Process” found in Electronic News, Jan. 20, 1997 issue. This reference is hereby incorporated by reference for purposes of explaining this particular type of imaging processor.
Another example of a recent development in solid state imaging is the development of CMOS imaging sensor which is able to achieve analog to digital conversion on each of the pixels within the pixel array. This type of improved CMOS imager includes transistors at every pixel to provide digital instead of analog output that enable the delivery of decoders and sense amplifiers much like standard memory chips. With this new technology, it may, therefore, be possible to manufacture a true digital “camera on a chip.” This CMOS imager has been developed by a Stanford University joint project and is headed by Professor Abbas el-Gamal.
A second approach to creating a CMOS-based digital imaging device includes the use of an over-sample converter at each pixel with a one bit comparator placed at the edge of the pixel array instead of performing all of the analog to digital functions on the pixel. This new design technology has been called MOSAD (multiplexed over sample analog to digital) conversion. The result of this new process is low power usage, along with the capability to achieve enhanced dynamic range, possibly up to 20 bits. This process has been developed by Amain Electronics of Simi Valley, Calif. A brief description of both of the processes developed by Stanford University and Amain Electronics can be found in an article entitled “A/D Conversion Revolution for CMOS Sensor?,” September 1998 issue of Advanced Imaging. This reference is also hereby incorporated by reference for purposes of explaining these particular types of imaging processors.
The above-mentioned developments in solid state imaging technology have shown that “camera on a chip” devices will continue to be enhanced not only in terms of the quality of imaging which may be achieved, but also in the specific construction of the devices which may be manufactured by new breakthrough processes.
Although the “camera on a chip” concept is one which has great merit for application in many industrial areas, a need still exists for a reduced area imaging device which can be used in even the smallest type of endoscopic instruments in order to view areas in the body that are particularly difficult to access, and to further minimize patient trauma by an even smaller diameter invasive instrument.
It is one object of this invention to provide reduced area imaging devices which take advantage of “camera on a chip” technology, but rearrange the circuitry in a stacked relationship so that there is a minimum profile presented when used within a surgical instrument or other investigative device. It is another object of this invention to provide low cost imaging devices which may be “disposable.” It is yet another object of this invention to provide reduced area imaging devices which may be used in conjunction with standard endoscopes by placing the imaging device through channels which normally receive other surgical devices, or receive liquids or gases for flushing a surgical area. It is yet another object of this invention to provide a surgical device with imaging capability which may be battery powered and only requires one conductor for transmitting a pre-video signal to video processing circuitry within or outside the sterile field of the surgical area.
It is yet another object of the invention to provide a reduced area imaging device which utilizes selected charge integration periods in order to enhance the image in terms of a desired brightness or intensity. In the treatment of cancer, fluorescent markers have been used to help identify cancerous tissue within a patient. One example of a prior art reference which discloses a method of detection and treatment of malignant and nonmalignant tumors is U.S. Pat. No. 5,211,938 to Kennedy et al. Specifically, this reference discloses a method of detection of malignant and non-malignant lesions by photo-chemotherapy of protoporphyrin IX precursors. 5-amino levulinic acid (5-ALA) is administered to the patient in an amount sufficient to induce synthesis of protoporphyrin IX in the lesions, followed by exposure of the treated lesion to a photo activating light in the range of 350–640 nanometers. Naturally occurring protoporphyrin IX is activatable by light in the incident red light range which more easily passes through human tissue as compared to light of other wave lengths. An endoscopic procedure may then be used to locate the photo activated lesions.
Other methods relating to cancer screening using fluorescence detection systems require the use of interventional devices such as endoscopes which have the special capability of delivering specified light frequencies to a targeted area within a patient. These endoscopes illuminate the targeted part of the body in which cancer is suspected. The light illuminates the targeted area which has previously been subjected to some type of fluorescent marker, causing the malignant cells to illuminate or fluoresce under observation of light at the specified frequency.
One distinct disadvantage or problem associated with use of fluorescent markers to locate and treat cancerous tissue is that it is oftentimes difficult to locate the cancerous tissue at all locations, particularly when lesions are at their early stages in formation, or the cancerous tissue has not yet grown to an extent which creates an observable amount of fluorescence. Furthermore, because an endoscopic procedure is undertaken to locate and treat many lesions, the surgeon does not have an infinite amount of time to locate or treat a particular lesion. Therefore, a need exists for enhancing observable fluorescence as well as being able to use an imager of such a small size that fluorescence endoscopy can be used in a wide array of surgical procedures.
In addition to the intended use of the foregoing invention with respect to medical purposes, it is also contemplated that the invention described herein has great utility with respect to oral surgery and general dental procedures wherein a very small imaging device can be used to provide an image of particularly difficult to access locations. Additionally, while the foregoing invention has application with respect to the medical and dental fields, it will also be appreciated by those skilled in the art that the small size of the imaging device set forth herein can be applied to other functional disciplines wherein the imaging device can be used to view difficult to access locations for industrial equipment and the like. Therefore, the imaging device of this invention could be used to replace many industrial boroscopes.
The “camera on a chip” technology can be furthered improved with respect to reducing its profile area and incorporating such a reduced area imaging device into very small investigative instruments which can be used in the medical, dental, or other industrial fields.
In accordance with the present invention, reduced area imaging devices are provided. The term “imaging device” as used herein describes the imaging elements and processing circuitry which is used to produce a video signal which may be accepted by a standard video device such as a television or video monitor accompanying a personal computer. The term “image sensor” as used herein describes the components of a solid state imaging device which captures images and stores them within the structure of each of the pixels in the array of pixels found in the imaging device. As further discussed below, the timing and control circuits can be placed either on the same planar structure as the pixel array, in which case the image sensor can also be defined as an integrated circuit, or the timing and control circuitry can be placed remote from the pixel array. The terms “signal” or “image signal” as used herein, and unless otherwise more specifically defined, refer to an image which at some point during its processing by the imaging device, is found in the form of electrons which have been placed in a specific format or domain. The term “processing circuitry” as used herein refers to the electronic components within the imaging device which receive the image signal from the image sensor and ultimately place the image signal in a usable format. The terms “timing and control circuits” or “circuitry” as used herein refer to the electronic components which control the release of the image signal from the pixel array.
In a first embodiment, the image sensor, with or without the timing and control circuitry, may be placed at the distal tip of the endoscopic instrument while the remaining processing circuitry may be found in a small remote control box which may communicate with the image sensor by a single cable.
In a second embodiment, the image sensor and the processing circuitry may all be placed in a stacked arrangement of circuit boards and positioned at the distal tip of the endoscopic instrument. In this embodiment, the pixel array of the image sensor may be placed by itself on its own circuit board while the timing and control circuitry and processing circuitry are placed on one or more other circuit boards. Alternatively, the circuitry for timing and control may be placed with the pixel array on one circuit board, while the remaining processing circuitry can be placed on one or more of the other circuit boards.
In another embodiment, the imaging device may be adapted for use with a standard rod lens endoscope wherein the imaging device is placed within a standard camera housing which is configured to connect to a standard “C” or “V” mount connector.
In yet another embodiment, the imaging device may be configured so that the processing circuitry is placed in the handle of the endoscope, which eliminates the necessity of having a remote box when the processing circuitry is remote from the pixel array. In this embodiment, the pixel array and the timing and control circuitry are placed at the distal tip of the endoscopic instrument, while the processing circuitry is placed within the handle of the endoscope.
For each of the embodiments, selected charge integration periods may be used to enhance the image to a desired brightness or intensity. Particularly in the field of medical fluorescence detection, the ability to adjust charge integration periods greatly enhances the ability to observe fluorescence from a group of cells which might otherwise be unobservable with normal or preset integration periods.
While the imager may be used within an endoscopic instrument, it is also contemplated that the image sensor may be incorporated within a microscope, or another imaging device which is used to view cell cultures and the like. Most commonly available fluorescence microscopes include CCD type imagers which are not capable of the variable charge integration. CCD imagers are charge storage and transfer devices wherein the detector signal produced is representative of the total light impinging or falling upon the pixel array during a preset exposure time. Because of the construction of CCD devices, these exposure times cannot be manipulated for charge integration because CCD imagers have destructive readout. In other words, each charge is read by transferring the collected charge in each pixel in a serial fashion to a readout amplifier. The same photon generated charge collected at the pixel site is transferred (coupled) pixel by pixel, one at a time, in a predesignated sequence that cannot be interrupted. When the pixel charge sequence is transferred to the readout amplifier, the pixel charge is destroyed. For CID (charge injection device) imagers, pixels accumulate charge which is injected into the substrate. Pixels in CID imagers can be individually accessed; however, in doing so, the charge is not destroyed by actual charge transfer, but is sensed and then replaced so that the integration process is not disturbed. Light continues to be collected for the preset integration period while the pixels continue to be monitored. This nondestructive readout capability of CID imagers makes it possible to carry out real time exposure monitoring and it also allows integration periods to be varied such that longer integration periods represent greater amounts of light being collected in the pixels.
By having the capability to adjust the integration periods, fluorescence detection can be enhanced by choosing an integration time which maximizes observable fluorescence. CMOS imagers also have variable charge integration capability to enhance observed fluorescence. As with CID imagers, integration periods in CMOS imagers may be varied, and fluorescence detection can be enhanced by choosing an integration period which maximizes the same. These CMOS imagers, as well as commercially available CMOS-CID imagers such as those manufactured by CIDTEC of Liverpool, NY can be modified to include an imager integration time select switch which allows an operator to preselect a desired integration period which maximizes observable fluorescence. The imagers sold by CIDTEC are “camera on a chip” type CMOS devices. The imager integration time select switch is coupled to video processing circuitry by clock select circuitry which varies the integration period as selected by the operator. Representative integration periods might include 250 milliseconds, 500 milliseconds, 2 seconds, 3 seconds and 5 seconds. The operator would adjust the integration periods to maximize the observed fluorescence. For example, an integration period selected at 5 seconds would result in charge being accumulated in the pixels of the imager for a 5-second period and thus, the observed fluorescence intensity would be greatly increased in comparison to standard readout cycles for CCD devices which may only be one-sixtieth of a second.
In a CMOS-CID device, photon charge collected by the photo-diodes are injected into the pixel substrate and stored. The photo-diodes continue to collect charge and transfers the charge into the substrate. The charge stored in the substrate continues to accumulate from the photo-diodes until the chosen integration period ends (i.e., the integration period selected by the user). At that time, the pixels are read out and the integration process begins again. Readout clock select circuitry creates a frequency which is fed into a series of CMOS divider circuits which divide the clock frequency down to a user selected clock rate. The user selected clock rate would correspond to the select switch positions enabling the operator to have a choice of a plurality of integration time periods. Because CMOS pixels can be accessed individually, the image can be updated as desired through various update cycles within the display monitor, while continuing to wait for the read out signal from the imager without disturbing the selected integration period. The user selectable integration time switch can be mounted as desired based upon the particular configuration of the imaging device. In the configuration of the imaging device which may utilize a control box, the integration time switch could be mounted on the front panel of the control box, and the additional circuitry required for charge integration would simply be incorporated within the control box. In the configuration of the imaging device in which all of the processing circuitry is housed within the particular endoscope or other instrument, the switch could simply be mounted on the handle of the instrument. Published papers which provide good background information on charge injection devices include “Charge Injection Devices for Use in Astronomy”, by Z. Ninkov et al., SPIE Proceedings, 1994, Publication No. 2198, Vol. 868; and “Evaluation of a Charge Injection Device Array”, by Z. Ninkov et al., SPIE Proceedings, 1994, Publication No. 2172, Vol. 15. These two papers are hereby incorporated by reference.
For use of the imaging device in endoscopy, a generic endoscope may be used which includes a very small diameter tubular portion which is inserted within the patient. The tubular portion may be made of a flexible material having a central lumen or opening therein for receiving the elements of the imaging device. The tubular portion may be modified to include an additional concentric tube placed within the central lumen and which enables a plurality of light fibers to be placed circumferentially around the periphery of the distal end of the tubular portion. Additionally, control wires may extend along the tubular portion in order to make the endoscope steerable. The material used to make the endoscope can be compatible with any desired sterilization protocol, or the entire endoscope can be made sterile and disposable after use.
For the configuration of the imaging device which calls for the array of pixels and the timing and control circuitry to be placed on the same circuit board, only one conductor is required in order to transmit the image signal to the processing circuitry. In the other configuration of the imaging device wherein the timing and control circuits are incorporated onto other circuit boards, a plurality of connections are required in order to connect the timing and control circuitry to the pixel array and the one conductor is also required to transmit the image signal.
In addition to use of the imaging device in endoscopy, it is also contemplated that the imaging device of the invention can be incorporated within a microscope which may be used to analyze cell cultures and the like. Although size is not as much of a concern with use of the imaging device within a microscope, there are still great advantages to be obtained by providing the imaging device with selected charge integration periods to intensify the brightness of an image in fluorescence detection of cell culture media which has no observable fluorescence as observed under standard integration periods.
In accordance with one embodiment of the invention as shown in
An image sensor 40 may be placed within the central channel defined by inner tube 20. In the configuration shown in
A control box 30 may be placed remote from the endoscope 10. The control box 30 contains some of the processing circuitry which is used to process the image signal produced by image sensor 40. Therefore, the imaging device 11 as previously defined would include the processing circuitry within control box 30 and the image sensor 40 located at the distal tip of the endoscope. Control box 30 communicates with image sensor 40 by means of cable 32 which may simply be an insulated and shielded cable which houses therein cable 26. Cable 32 is stabilized with respect to the handle portion 12 by means of a fitting 34 which ensures that cable 32 cannot be inadvertently pushed or pulled within channel 13. Additionally, an additional fitting 35 may be provided to stabilize the entry of a light cable 36 which houses the plurality of light fibers 22.
Image sensor 40 is illustrated as being a planar and square shaped member. However, the image sensor may be modified to be in a planar and circular shape to better fit within the channel defined by inner tube 20. Accordingly,
Image sensor 40 can be as small as 1 mm in its largest dimension. However, a more preferable size for most endoscopic procedures would dictate that the image sensor 40 be between 4 mm to 8 mm in its largest dimension. The image signal transmitted from the image sensor through conductor 48 is also herein referred to as a pre-video signal. Once the pre-video signal has been transmitted from image sensor 40 by means of conductor 48, it is received by video processing board 50. Video processing board 50 then carries out all the necessary conditioning of the pre-video signal and places it in a form so that it may be viewed directly on a standard video device, television or standard computer video monitor. The signal produced by the video processing board 50 can be further defined as a post-video signal which can be accepted by a standard video device. As shown in
As shown in
Referring back to the handle portion 12 in
In the first embodiment illustrated in
Optionally, a supplementary processing board 60 may be provided to further enhance the pre-video signal. As shown in
Although the active pixel array disclosed in U.S. Pat. No. 5,471,515 is mentioned herein, it will be understood that the hybrid CCD/CMOS described above, or any other solid state imaging device may be used wherein timing and control circuits can be placed either on the same planar structure with the pixel array, or may be separated and placed remotely. Furthermore, it will be clearly understood that the invention claimed herein is not specifically limited to an image sensor as disclosed in the U.S. Pat. No. 5,471,515, but encompasses any image sensor which may be configured for use in conjunction with the other processing circuitry which makes up the imaging device of this invention.
The timing and control circuits 92 are used to control the release of the image information or image signal stored in the pixel array. In the image sensor of Fossum, et al., the pixels are arranged in a plurality of rows and columns. The image information from each of the pixels is first consolidated in a row by row fashion, and is then downloaded from one or more columns which contain the consolidated information from the rows. As shown in
The information released from the column or columns is also controlled by a series of latches 102, a counter 104 and a decoder 106. As with the information from the rows, the column information is also placed in a serial format which may then be sent to the video processing board 50. This serial format of column information is the pre-video signal carried by conductor 48. The column signal conditioner 108 places the column serial information in a manageable format in the form of desired voltage levels. In other words, the column signal conditioner 108 only accepts desired voltages from the downloaded column(s).
The clock input to the timing and control circuits 92 may simply be a quartz crystal timer. This clock input is divided into many other frequencies for use by the various counters. The run input to the timing and control circuit 92 may simply be an on/off control. The default input can allow one to input the pre-video signal to a video processor board which may run at a frequency of other than 30 hertz. The data input controls functions such as zoom. At least for a CMOS type active pixel array which can be accessed in a random manner, features such as zoom are easily manipulated by addressing only those pixels which locate a desired area of interest by the surgeon.
A further discussion of the timing and control circuitry which may be used in conjunction with an active pixel array is disclosed in U.S. Pat. No. 5,471,515 and is also described in an article entitled “Active Pixel Image Sensor Integrated With Readout Circuits” appearing in NASA Tech Briefs, October 1996, pp. 38 and 39. This particular article is also incorporated by reference.
Once image sensor 40 has created the pre-video signal, it is sent to the video processing board 50 for further processing. At board 50, as shown in
Referring to the output of the white balance circuit 124, this chroma portion of the signal is sent to a delay line 126 where the signal is then further reduced by switch 128. The output of switch 128 is sent through a balanced modulator 130 and also to the Y chroma mixer 132 where the processed chroma portion of the signal is mixed with the processed non-chroma portion. Finally, the output from the Y chroma mixer 132 is sent to the NTSC/PAL encoder 134, commonly known in the art as a “composite” encoder. The composite frequencies are added to the signal leaving the Y chroma mixer 132 in encoder 134 to produce the post-video signal which may be accepted by a television.
Referring back to
In addition to digital enhancement, supplementary board 60 may further include other circuitry which may further condition the post-video signal so that it may be viewed in a desired format other than NTSC/PAL. As shown in
The next encoder illustrated in
One difference between the arrangement of image sensor 40 and the outputs found in FIG. 3 of the Fossum, et al. patent is that in lieu of providing two analog outputs [namely, VS out (signal) and VR out (reset)], the reset function takes place in the timing and control circuitry 92. Accordingly, the pre-video signal only requires one conductor 48.
As shown in
The next major element is the automatic gain control 140 shown in
Digital signal processor 144 of
After the signal is processed by digital signal processor 144, the signal is sent to digital encoder 148 illustrated in
This reconverted analog signal is then buffered at buffers 151 and then sent to amplifier group 152 of
In addition to the active pixel-type CMOS imager discussed above, certain advances in passive pixel-type CMOS imagers have been made such that the traditional noise associated with such passive arrangements can be overcome by improved manufacturing technologies which therefore does not require each signal to be amplified at each pixel site. Accordingly,
As seen in
It should be understood that the imager 40 may be used in conjunction with the optics of a fluorescence microscope. Many fluorescence microscopes today also have miniature cameras which are used to record images observed by the fluorescence microscope. Thus, the imager 40 could replace the miniature camera or imager used on commercially available fluorescence microscopes. Also, it shall be understood that an endoscope which may be used in fluorescence guided endoscopy may also incorporate variable charge integration capability in order to enhance the ability to find and evaluate fluorescing cells. Thus, the use of variable charge integration capability has multiple benefits not only in viewing cells which have been removed from a body, but also to view cells in the body which may undergo some treatment or surgical procedure, and are to be located by fluorescence guided endoscopy.
Fluorescence-assisted surgery and fluorescence-assisted endoscopy can also be enhanced by providing an endoscope utilizing a CMOS-CID imager which has variable charge integration capability. The ability of a surgeon to view a cancerous growth inside the patient can be enhanced by choosing an integration period which greatly expands the imaging sensitivity of the endoscope. The faint or slight amount of fluorescence which might not be observable through a CCD imager can be enhanced by using a CMOS-CID imager modified with variable charge integration capability, resulting in readily observable fluorescence. Thus, in every conceivable aspect of endoscopy and cancer screening, use of an endoscope having a variable charge integration capability is advantageous for finding a cancerous growth.
One example of fluorescence guided endoscopy might be fluorescence endoscopy to find colon cancer. Once the patient has been administered 5-ALA or another similar compound, the surgeon would conduct the endoscopic procedure looking for fluorescing colon tissue. As the surgeon conducts the endoscopic procedure, the charge integration periods could be adjusted to maximize observable fluorescence. In some cases, it may be very difficult for the surgeon to find all fluorescing tissues within the colon. By using the variable charge integration capability incorporated within the endoscope, the surgeon is more capable of finding each and every fluorescing groups of tissue within the colon to make a proper diagnosis. Also, light delivery to the surgical site can be chosen from a desired frequency of light corresponding to the excitation frequency of the compound administered to the patient.
From the foregoing, it is apparent that an entire imaging device may be incorporated within the distal tip of an endoscope, or may have some elements of the imaging device being placed in a small remote box adjacent to the endoscope. Based upon the type of image sensor used, the profile area of the imaging device may be made small enough to be placed into an endoscope which has a very small diameter tube. Additionally, the imaging device may be placed into the channels of existing endoscopes to provide additional imaging capability without increasing the size of the endoscope. The imaging device may be powered by a standard power input connection in the form of a power cord, or a small lithium battery may be used.
The imaging device of the invention can be further enhanced by incorporating a charge integration feature which enhances the ability of a user to selectively adjust the brightness of an image. As discussed above, fluorescence detection in patient screening and treatment for a wide array of photo-dynamic treatments can be greatly improved by utilizing the imaging device of the invention having charge integration capability.
This invention has been described in detail with reference to particular embodiments thereof, but it will be understood that various other modifications can be effected within the spirit and scope of this invention.
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|U.S. Classification||348/76, 348/65, 348/E03.019, 348/E05.027, 348/68, 257/E25.032|
|International Classification||H04N5/374, H04N5/228, H04N5/353, H01L25/16, H04N5/225, A61B1/05, A61B1/005, H04N7/18|
|Cooperative Classification||A61B1/043, A61B1/00096, A61B1/07, A61B1/05, H04N2005/2255, H04N5/374, A61B1/00135, A61B1/0051, A61B1/0607, H01L25/167, H01L2924/3011, H04N5/2253, H04N5/353, H01L2924/0002|
|European Classification||A61B1/00H4, A61B1/06B, A61B1/00E4H7, H04N5/374, H04N5/353, H04N5/225C3, H01L25/16L, A61B1/05|
|Jan 18, 2002||AS||Assignment|
Owner name: MICRO-MEDICAL DEVICES, INC., COLORADO
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:ADAIR, EDWIN L.;ADAIR, JEFFREY L.;ADAIR, RANDALL S.;REEL/FRAME:012515/0361
Effective date: 20011102
|Nov 17, 2005||AS||Assignment|
Owner name: MICRO-IMAGING SOLUTIONS, INC., COLORADO
Free format text: CHANGE OF NAME;ASSIGNOR:MICRO-MEDICAL DEVICES, INC.;REEL/FRAME:016793/0057
Effective date: 20050921
|Jul 6, 2009||FPAY||Fee payment|
Year of fee payment: 4
|Mar 11, 2013||FPAY||Fee payment|
Year of fee payment: 8